Loading…

Human skin permeation of Δ8-tetrahydrocannabinol, cannabidiol and cannabinol

ABSTRACT The purpose of this study was to quantify the in‐vitro human skin transdermal flux of Δ8‐tetrahydrocannabinol (Δ8‐THC), cannabidiol (CBD) and cannabinol (CBN). These cannabinoids are of interest because they are likely candidates for transdermal combination therapy. Differential thermal ana...

Full description

Saved in:
Bibliographic Details
Published in:Journal of pharmacy and pharmacology 2004-03, Vol.56 (3), p.291-297
Main Authors: Stinchcomb, Audra L., Valiveti, Satyanarayana, Hammell, Dana C., Ramsey, Diana R.
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c2039-74a5d08cd854ed399c3a1d2e4b85a164eff4cea8efc1ccb3469eb103d69c6dbb3
cites cdi_FETCH-LOGICAL-c2039-74a5d08cd854ed399c3a1d2e4b85a164eff4cea8efc1ccb3469eb103d69c6dbb3
container_end_page 297
container_issue 3
container_start_page 291
container_title Journal of pharmacy and pharmacology
container_volume 56
creator Stinchcomb, Audra L.
Valiveti, Satyanarayana
Hammell, Dana C.
Ramsey, Diana R.
description ABSTRACT The purpose of this study was to quantify the in‐vitro human skin transdermal flux of Δ8‐tetrahydrocannabinol (Δ8‐THC), cannabidiol (CBD) and cannabinol (CBN). These cannabinoids are of interest because they are likely candidates for transdermal combination therapy. Differential thermal analysis and in‐vitro diffusion studies with human tissue were completed for the compounds. Heats of fusion, melting points and relative thermodynamic activities were determined for the crystalline compounds, CBD and CBN. Flux, permeability, tissue concentration and lag times were measured in the diffusion experiments. CBN had a lower heat of fusion and corresponding higher calculated relative thermodynamic activity than CBD. Ethanol concentrations of 30 to 33% significantly increased the transdermal flux of Δ8‐THC and CBD. Tissue concentrations of Δ8‐THC were significantly higher than for CBN. Lag times for CBD were significantly smaller than for CBN. The permeabilities of CBD and CBN were 10‐fold higher than for Δ8‐THC. Combinations of these cannabinoids with ethanol will be further studied in transdermal patch formulations in vitro and in vivo, as significant flux levels of all the drugs were obtained. CBD, the most polar of the three drugs, and other more polar cannabinoids will also be the focus of future drug design studies for improved transdermal delivery rates.
doi_str_mv 10.1211/0022357022791
format article
fullrecord <record><control><sourceid>istex_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1211_0022357022791</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_861FL5CB_G</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2039-74a5d08cd854ed399c3a1d2e4b85a164eff4cea8efc1ccb3469eb103d69c6dbb3</originalsourceid><addsrcrecordid>eNp9kM1KAzEQx4MoWKtH73kAo_nYfOxRi22Vqj0oHkM2yWLsNluSFdv38Ll8JltaLF68zAz8fjMDfwDOCb4klJArjCllXK6rLMkB6FFcUCQJV4egt2FoDdkxOMn5HWMshRA98DD-mJsI8yxEuPBp7k0X2gjbGn5_KdT5Lpm3lUutNTGaKsS2uYC72YW2gSY6uGen4Kg2TfZnu94HL8Pb58EYTZ5Gd4PrCbIUsxLJwnCHlXWKF96xsrTMEEd9USluiCh8XRfWG-VrS6ytWCFKXxHMnCitcFXF-gBt79rU5px8rRcpzE1aaYL1Jgv9J4u1z7b-Z2j86n9Z30_HUypwuf8ScueXv1smzbSQTHL9-jjSSpDhhA9u9Ij9AKMTcKY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Human skin permeation of Δ8-tetrahydrocannabinol, cannabidiol and cannabinol</title><source>Oxford Journals Online</source><creator>Stinchcomb, Audra L. ; Valiveti, Satyanarayana ; Hammell, Dana C. ; Ramsey, Diana R.</creator><creatorcontrib>Stinchcomb, Audra L. ; Valiveti, Satyanarayana ; Hammell, Dana C. ; Ramsey, Diana R.</creatorcontrib><description>ABSTRACT The purpose of this study was to quantify the in‐vitro human skin transdermal flux of Δ8‐tetrahydrocannabinol (Δ8‐THC), cannabidiol (CBD) and cannabinol (CBN). These cannabinoids are of interest because they are likely candidates for transdermal combination therapy. Differential thermal analysis and in‐vitro diffusion studies with human tissue were completed for the compounds. Heats of fusion, melting points and relative thermodynamic activities were determined for the crystalline compounds, CBD and CBN. Flux, permeability, tissue concentration and lag times were measured in the diffusion experiments. CBN had a lower heat of fusion and corresponding higher calculated relative thermodynamic activity than CBD. Ethanol concentrations of 30 to 33% significantly increased the transdermal flux of Δ8‐THC and CBD. Tissue concentrations of Δ8‐THC were significantly higher than for CBN. Lag times for CBD were significantly smaller than for CBN. The permeabilities of CBD and CBN were 10‐fold higher than for Δ8‐THC. Combinations of these cannabinoids with ethanol will be further studied in transdermal patch formulations in vitro and in vivo, as significant flux levels of all the drugs were obtained. CBD, the most polar of the three drugs, and other more polar cannabinoids will also be the focus of future drug design studies for improved transdermal delivery rates.</description><identifier>ISSN: 0022-3573</identifier><identifier>EISSN: 2042-7158</identifier><identifier>DOI: 10.1211/0022357022791</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><ispartof>Journal of pharmacy and pharmacology, 2004-03, Vol.56 (3), p.291-297</ispartof><rights>2004 Royal Pharmaceutical Society of Great Britain</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2039-74a5d08cd854ed399c3a1d2e4b85a164eff4cea8efc1ccb3469eb103d69c6dbb3</citedby><cites>FETCH-LOGICAL-c2039-74a5d08cd854ed399c3a1d2e4b85a164eff4cea8efc1ccb3469eb103d69c6dbb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Stinchcomb, Audra L.</creatorcontrib><creatorcontrib>Valiveti, Satyanarayana</creatorcontrib><creatorcontrib>Hammell, Dana C.</creatorcontrib><creatorcontrib>Ramsey, Diana R.</creatorcontrib><title>Human skin permeation of Δ8-tetrahydrocannabinol, cannabidiol and cannabinol</title><title>Journal of pharmacy and pharmacology</title><description>ABSTRACT The purpose of this study was to quantify the in‐vitro human skin transdermal flux of Δ8‐tetrahydrocannabinol (Δ8‐THC), cannabidiol (CBD) and cannabinol (CBN). These cannabinoids are of interest because they are likely candidates for transdermal combination therapy. Differential thermal analysis and in‐vitro diffusion studies with human tissue were completed for the compounds. Heats of fusion, melting points and relative thermodynamic activities were determined for the crystalline compounds, CBD and CBN. Flux, permeability, tissue concentration and lag times were measured in the diffusion experiments. CBN had a lower heat of fusion and corresponding higher calculated relative thermodynamic activity than CBD. Ethanol concentrations of 30 to 33% significantly increased the transdermal flux of Δ8‐THC and CBD. Tissue concentrations of Δ8‐THC were significantly higher than for CBN. Lag times for CBD were significantly smaller than for CBN. The permeabilities of CBD and CBN were 10‐fold higher than for Δ8‐THC. Combinations of these cannabinoids with ethanol will be further studied in transdermal patch formulations in vitro and in vivo, as significant flux levels of all the drugs were obtained. CBD, the most polar of the three drugs, and other more polar cannabinoids will also be the focus of future drug design studies for improved transdermal delivery rates.</description><issn>0022-3573</issn><issn>2042-7158</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNp9kM1KAzEQx4MoWKtH73kAo_nYfOxRi22Vqj0oHkM2yWLsNluSFdv38Ll8JltaLF68zAz8fjMDfwDOCb4klJArjCllXK6rLMkB6FFcUCQJV4egt2FoDdkxOMn5HWMshRA98DD-mJsI8yxEuPBp7k0X2gjbGn5_KdT5Lpm3lUutNTGaKsS2uYC72YW2gSY6uGen4Kg2TfZnu94HL8Pb58EYTZ5Gd4PrCbIUsxLJwnCHlXWKF96xsrTMEEd9USluiCh8XRfWG-VrS6ytWCFKXxHMnCitcFXF-gBt79rU5px8rRcpzE1aaYL1Jgv9J4u1z7b-Z2j86n9Z30_HUypwuf8ScueXv1smzbSQTHL9-jjSSpDhhA9u9Ij9AKMTcKY</recordid><startdate>200403</startdate><enddate>200403</enddate><creator>Stinchcomb, Audra L.</creator><creator>Valiveti, Satyanarayana</creator><creator>Hammell, Dana C.</creator><creator>Ramsey, Diana R.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200403</creationdate><title>Human skin permeation of Δ8-tetrahydrocannabinol, cannabidiol and cannabinol</title><author>Stinchcomb, Audra L. ; Valiveti, Satyanarayana ; Hammell, Dana C. ; Ramsey, Diana R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2039-74a5d08cd854ed399c3a1d2e4b85a164eff4cea8efc1ccb3469eb103d69c6dbb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stinchcomb, Audra L.</creatorcontrib><creatorcontrib>Valiveti, Satyanarayana</creatorcontrib><creatorcontrib>Hammell, Dana C.</creatorcontrib><creatorcontrib>Ramsey, Diana R.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Journal of pharmacy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stinchcomb, Audra L.</au><au>Valiveti, Satyanarayana</au><au>Hammell, Dana C.</au><au>Ramsey, Diana R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human skin permeation of Δ8-tetrahydrocannabinol, cannabidiol and cannabinol</atitle><jtitle>Journal of pharmacy and pharmacology</jtitle><date>2004-03</date><risdate>2004</risdate><volume>56</volume><issue>3</issue><spage>291</spage><epage>297</epage><pages>291-297</pages><issn>0022-3573</issn><eissn>2042-7158</eissn><abstract>ABSTRACT The purpose of this study was to quantify the in‐vitro human skin transdermal flux of Δ8‐tetrahydrocannabinol (Δ8‐THC), cannabidiol (CBD) and cannabinol (CBN). These cannabinoids are of interest because they are likely candidates for transdermal combination therapy. Differential thermal analysis and in‐vitro diffusion studies with human tissue were completed for the compounds. Heats of fusion, melting points and relative thermodynamic activities were determined for the crystalline compounds, CBD and CBN. Flux, permeability, tissue concentration and lag times were measured in the diffusion experiments. CBN had a lower heat of fusion and corresponding higher calculated relative thermodynamic activity than CBD. Ethanol concentrations of 30 to 33% significantly increased the transdermal flux of Δ8‐THC and CBD. Tissue concentrations of Δ8‐THC were significantly higher than for CBN. Lag times for CBD were significantly smaller than for CBN. The permeabilities of CBD and CBN were 10‐fold higher than for Δ8‐THC. Combinations of these cannabinoids with ethanol will be further studied in transdermal patch formulations in vitro and in vivo, as significant flux levels of all the drugs were obtained. CBD, the most polar of the three drugs, and other more polar cannabinoids will also be the focus of future drug design studies for improved transdermal delivery rates.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1211/0022357022791</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0022-3573
ispartof Journal of pharmacy and pharmacology, 2004-03, Vol.56 (3), p.291-297
issn 0022-3573
2042-7158
language eng
recordid cdi_crossref_primary_10_1211_0022357022791
source Oxford Journals Online
title Human skin permeation of Δ8-tetrahydrocannabinol, cannabidiol and cannabinol
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T05%3A38%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Human%20skin%20permeation%20of%20%CE%948-tetrahydrocannabinol,%20cannabidiol%20and%20cannabinol&rft.jtitle=Journal%20of%20pharmacy%20and%20pharmacology&rft.au=Stinchcomb,%20Audra%20L.&rft.date=2004-03&rft.volume=56&rft.issue=3&rft.spage=291&rft.epage=297&rft.pages=291-297&rft.issn=0022-3573&rft.eissn=2042-7158&rft_id=info:doi/10.1211/0022357022791&rft_dat=%3Cistex_cross%3Eark_67375_WNG_861FL5CB_G%3C/istex_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c2039-74a5d08cd854ed399c3a1d2e4b85a164eff4cea8efc1ccb3469eb103d69c6dbb3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true